Two years ago today I went by myself, to the opticians, for what I thought was just a 2-yearly check-up. 10 minutes into my appointment, and Stargardts had changed my life forever.
2 years on and although I have devastatingly already lost 2 lines of the eye chart in both eyes and there is deterioration on my scan pictures (although I am hoping with all I have that my eyes get slightly better once my baby is here) I am continuing to try and stay as positive as I can, but it’s not always easy. You can never get away from vision loss, you look through it all of the time and it is with you every waking minute of the day to remind you of what you have lost and what you are still to lose. Your eyes constantly have to adjust from one light setting to another, from one season to the next, no eye day is the same and this can be frustrating.
People always say to me how well I have done to carry on, but there was no other option, this isn’t a fixable situation, so I just have the make the best of what I still have.
In 2 years I have had so much support from my close family and friends and also from the network I created for myself online to help me cope and I am extremely grateful to every one of those people who help lift me up when I feel down and help me to feel less alone with something so rare. There are also others who have just disregarded my Stargardts like it’s a twisted ankle and make me feel like I should just ‘get over it’, without any thought to how they may feel or cope being in my situation. People forget its progressive and realistically, by the time I am pushing 50, I probably won’t have much, if any central vision left and of course that could be even earlier as nobody knows the progression (unless a cure is found in that time 🤞🏼). Regardless of the latter, I am proud of how far I have come in the 2 years since my Stargardts was discovered and I am adamant I won’t let it stop me enjoying my life. I can’t deny that if I overthink my situation some days, fear grips me tightly and I will be honest and say I do get scared for my future and what I will miss, but none of us know what is around the corner and where we will be in ten year’s time, let alone tomorrow, so that’s why I try so hard to live for the now and for the moment, however big or small those moments might be and that is where Stargardts has changed my life for the better as I never did this before. If Stargardts has taught me anything, it’s that’s life is fragile, and things can change in a second and we should spend more time enjoying the small things and trying to let go of the things we can’t change and accepting them for what they are.
I never dreamed this would be my future and if I could change it I would in a heartbeat, but I can’t, so I can’t waste all my time dwelling on it. My biggest regret is letting anxiety take my twenties and manipulate what I could and couldn’t enjoy and after finally overcoming it and feeling so much better, A few months later I then got told I had Stargardts, but I don’t want that to take my 30’s and the rest of my life because this one isn’t fixable and life is too precious to waste on something I can’t control. There will be times where sadness consumes me with every time my eyes deteriorate, but I will get through it with the help of everyone around me and hopefully each year that passes, this day will become easier and more of a distant memory ♥️.
7 comments
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Bravo, Katie! We celebrate some anniversaries and, as your quote from Lynn Redgrave says, mourn others. This is not a diagnosis anyone needs to hear alone, but we all go to the doctor alone. I hope he was kind.
You don’t want to hear platitudes today or how well you are doing. Please know that many of us care. Sandy says she understands how, as a mom, today would feel to you.
You and your family are about to be blessed, and that makes today more emotional. Know that the one certainty is that your family will accept your love and return it to you. Sandy and I wish you all the joy in the world.
You have a great out look. Hm. Pun not intended! I understand where you’re coming from. I have a brain tumor that’s shortening my life and might be affecting my vision.
The hardest things we face are those that we have no control over. It’s so easy for others to tell us to just accept them, but they’re not the ones living with them.
Ultimately, we choose how to enjoy the time we have, whether it’s worrying or making our best life. It sounds like you are doing your best and that you are a pretty tough lady.
All my best.
Thank you so much Cindy, and I’m so sorry to hear of your brain tumour ❤️ life can be unfair sometimes, but we have to make the best of what we have, we have to keep fighting. All the best to you, another tough lady I’m sure xx
This is such an inspiring read. I am so sorry you are going through this but I love your determination to not let it ruin your life.
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Thank you so much ❤️